![n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja068057u/asset/images/large/ja068057un00001.jpeg)
n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society
![R)‐BINOL‐6,6'‐bistriflone: Shortened Synthesis, Characterization, and Enantioselective Catalytic Applications - Mouhtady - 2021 - European Journal of Organic Chemistry - Wiley Online Library R)‐BINOL‐6,6'‐bistriflone: Shortened Synthesis, Characterization, and Enantioselective Catalytic Applications - Mouhtady - 2021 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/e6157180-f322-4d98-9282-02658330cc2c/ejoc202101137-fig-5001-m.jpg)
R)‐BINOL‐6,6'‐bistriflone: Shortened Synthesis, Characterization, and Enantioselective Catalytic Applications - Mouhtady - 2021 - European Journal of Organic Chemistry - Wiley Online Library
ortho-Lithiations Reassessed: the Advantages of Deficiency Catalysis in Hydrocarbon Media | Organometallics
![A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB06910E A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB06910E](https://pubs.rsc.org/image/article/2012/OB/c2ob06910e/c2ob06910e-s1.gif)
A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C2OB06910E
![29 Si CPMAS NMR spectra of (a) carrier C, (b) C treated with BuLi, and... | Download Scientific Diagram 29 Si CPMAS NMR spectra of (a) carrier C, (b) C treated with BuLi, and... | Download Scientific Diagram](https://www.researchgate.net/profile/Eero_Iiskola2/publication/260663263/figure/fig4/AS:667714943205377@1536207056028/29-Si-CPMAS-NMR-spectra-of-a-carrier-C-b-C-treated-with-BuLi-and-c-C-treated-with_Q640.jpg)
29 Si CPMAS NMR spectra of (a) carrier C, (b) C treated with BuLi, and... | Download Scientific Diagram
![Concise synthesis of 3-alkylthieno[3,2- b ]thiophenes; building blocks for organic electronic and optoelectronic materials - RSC Advances (RSC Publishing) DOI:10.1039/C9RA08023F Concise synthesis of 3-alkylthieno[3,2- b ]thiophenes; building blocks for organic electronic and optoelectronic materials - RSC Advances (RSC Publishing) DOI:10.1039/C9RA08023F](https://pubs.rsc.org/image/article/2019/RA/c9ra08023f/c9ra08023f-s4_hi-res.gif)
Concise synthesis of 3-alkylthieno[3,2- b ]thiophenes; building blocks for organic electronic and optoelectronic materials - RSC Advances (RSC Publishing) DOI:10.1039/C9RA08023F
![NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d2e8dca2-ffa3-45ef-be98-0510dde7e2ee/anie202214106-fig-5002-m.jpg)
NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library
![A Rapid Injection NMR Study of the Reaction of Organolithium Reagents with Esters, Amides, and Ketones - ScienceDirect A Rapid Injection NMR Study of the Reaction of Organolithium Reagents with Esters, Amides, and Ketones - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1523706021109241-ol-2015-00650y_0005.jpg)